JPH061965A - Wet friction material - Google Patents

Wet friction material

Info

Publication number
JPH061965A
JPH061965A JP4185685A JP18568592A JPH061965A JP H061965 A JPH061965 A JP H061965A JP 4185685 A JP4185685 A JP 4185685A JP 18568592 A JP18568592 A JP 18568592A JP H061965 A JPH061965 A JP H061965A
Authority
JP
Japan
Prior art keywords
friction
resin
friction material
friction coefficient
fiber
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP4185685A
Other languages
Japanese (ja)
Other versions
JP3188311B2 (en
Inventor
Tatsuro Miyoshi
達朗 三好
Takashi Kitahara
俊 北原
Sakanori Umezawa
栄記 梅澤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NSK Warner KK
Original Assignee
NSK Warner KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NSK Warner KK filed Critical NSK Warner KK
Priority to JP18568592A priority Critical patent/JP3188311B2/en
Priority to US08/079,997 priority patent/US5395864A/en
Publication of JPH061965A publication Critical patent/JPH061965A/en
Application granted granted Critical
Publication of JP3188311B2 publication Critical patent/JP3188311B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16DCOUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D69/00Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
    • F16D69/02Composition of linings ; Methods of manufacturing
    • F16D69/025Compositions based on an organic binder
    • F16D69/026Compositions based on an organic binder containing fibres
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16DCOUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D2200/00Materials; Production methods therefor
    • F16D2200/0082Production methods therefor
    • F16D2200/0095Mixing an aqueous slurry of fibres with a binder, e.g. papermaking process

Landscapes

  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Braking Arrangements (AREA)

Abstract

PURPOSE:To provide the subject material high in its friction coefficient, good in stability of the friction coefficient, and excellent in heat resistance which comprises a fiber substrate, a filler, a thermosetting resin, and further active carbon fibers. CONSTITUTION:The objective material comprises (A) a fiber substrate such as a natural pulp fiber substrate or an organic synthetic fiber substrate, (B) a filler or a friction-controlling material such as diatomaceous earth or cashew nut resin, (C) a thermosetting synthetic resin, and (D) active carbon fibers. When a phenolic resin is used as the component C, the components A, B, C, and D are preferably compounded in a weight ratio of 20-60, 5-50, 10-40, and 1-40, respectively.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は、湿式摩擦係合装置に
おけるクラッチ及びブレーキに用いられる湿式摩擦材に
関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a wet friction material used for a clutch and a brake in a wet friction engagement device.

【0002】[0002]

【従来の技術】湿式摩擦係合装置の構成の一例を図6に
示す。図において、インプットシャフト6に嵌装された
ハブ5のスプライン部51に嵌合する駆動板2と、リテ
ーナ4のスプライン部41に嵌合する受動板1の接触に
より、トルクが伝達される。符号3はプレッシャープレ
ート、7は押圧のためのピストンである。
2. Description of the Related Art An example of the structure of a wet friction engagement device is shown in FIG. In the figure, torque is transmitted by contact between the drive plate 2 fitted to the spline portion 51 of the hub 5 fitted to the input shaft 6 and the passive plate 1 fitted to the spline portion 41 of the retainer 4. Reference numeral 3 is a pressure plate, and 7 is a piston for pressing.

【0003】このよううな摩擦係合装置に対しては、現
在エネルギー問題及び環境問題などからして小型軽量で
あること、作動ショックが小さいこと、及びトルク容量
の高いことが要求され、また自動車エンジンの高回転、
高出力化に伴う高エネルギー化に対しても同時に対応せ
ねばならず、その要求は極めて高いものである。
For such a friction engagement device, it is required at present that it is small and lightweight, has a small operating shock, and has a high torque capacity in view of energy problems and environmental problems. High rotation of
At the same time, it is necessary to simultaneously cope with the increase in energy accompanying the increase in output, and the demand is extremely high.

【0004】[0004]

【この発明が解決すべき課題】従来の摩擦係合装置にあ
っては、燃費低減のため、スリップ制御を採用したクラ
ッチの振動などの自励振動を抑制するため、潤滑油に摩
擦係数をさげる添加剤を配合し、対応している。また、
作動ショック低減のため、摩擦係数をさげる添加剤を配
合した潤滑油が多用されつつあり、小型化すれば必然的
に低トルク容量となってしまう。そのため作動押し力を
高くしてトルク容量を大きくするため、湿式摩擦材の剥
離寿命の低下、相手摩擦面(受動面)のヒートスポット
発生、及び熱変形、油圧ポンプの大型化、作動油の漏れ
などの耐久寿命に関する問題点、そしてこれらを解決す
るために安全率を考慮せねばならなくなり、装置自体の
小型化は困難であった。
In the conventional friction engagement device, in order to reduce fuel consumption, and to suppress self-excited vibration such as vibration of the clutch employing slip control, the friction coefficient is reduced in the lubricating oil. It is compatible with additives. Also,
In order to reduce the operational shock, lubricating oils containing an additive that lowers the friction coefficient are being used frequently, and miniaturization inevitably results in low torque capacity. Therefore, since the operating push force is increased to increase the torque capacity, the peeling life of the wet friction material is reduced, heat spots are generated on the friction surface of the other party (passive surface), thermal deformation, the hydraulic pump is upsized, and the hydraulic oil leaks. However, it has been difficult to reduce the size of the device itself, because it is necessary to consider the problems such as durability life and the safety factor in order to solve these problems.

【0005】従来技術においては、上記摩擦係合装置に
対応する摩擦材は、摩擦係数を高めようとすると、熱的
に不利となる傾向にあり、また耐熱性を求めると、摩擦
特性が悪化し、自励振動を発生させる問題があり、両立
させることは難しかった。
In the prior art, the friction material corresponding to the above-mentioned friction engagement device tends to be thermally disadvantageous if an attempt is made to increase the friction coefficient, and if heat resistance is required, the friction characteristics are deteriorated. However, there was a problem that self-excited vibration was generated, and it was difficult to achieve both at the same time.

【0006】[0006]

【課題を解決するための手段】この発明は前記のような
課題を解決するため、摩擦係数が高く、耐熱性に優れた
湿式摩擦材を得ようとするもので、摩擦材に繊維である
活性炭を含有させるようにしたものである。
In order to solve the above problems, the present invention intends to obtain a wet friction material having a high friction coefficient and excellent heat resistance. The friction material is activated carbon which is a fiber. Is included.

【0007】[0007]

【作用】比表面積の大きい活性炭を摩擦材に配合する
と、摩擦係数を下げる添加剤を選択的に吸着し、摩擦摺
動面において、摩擦係数を高める作用がある。またクラ
ッチ解放時においては、吸着した添加剤を放出し、潤滑
油内の添加剤の量に影響を与えることはない。この作用
は、活性炭の比表面積(多孔質であるため穴内部の表面
積を含む)を大きくすること(例えば2500m2
g)と、摩擦摺動面において活性炭接触面積を大きくす
ることの両立により効果が出る。
When the activated carbon having a large specific surface area is mixed with the friction material, it has the effect of selectively adsorbing the additive that lowers the friction coefficient and increasing the friction coefficient on the friction sliding surface. Further, when the clutch is released, the adsorbed additive is released and does not affect the amount of the additive in the lubricating oil. This action is to increase the specific surface area of the activated carbon (including the surface area inside the holes because it is porous) (eg 2500 m 2 /
The effect is obtained by satisfying both g) and increasing the activated carbon contact area on the friction sliding surface.

【0008】また、天然パルプ繊維、有機合成繊維等の
繊維基材と比べ熱伝導に優れ、配合することにより摩擦
熱を拡散し、相手摩擦板等の局部的な熱変態(ヒートス
ポットと呼ばれる)を防止する等によって、結果的に熱
的に有利な摩擦材を作り上げることができる。この発明
でいう繊維とは、繊維径が1μm〜50μm、繊維長が
0.1mm〜30mmをさし、摩擦材の配合割合は40
重量%以下の範囲が適当である。これ以上であると、価
格と性能の兼ね合いもあり、実用的ではない。
Further, it is superior in heat conduction to a fiber base material such as natural pulp fiber or organic synthetic fiber, and by blending it, frictional heat is diffused and local heat transformation (called a heat spot) of a mating friction plate or the like is called. As a result, a thermally advantageous friction material can be produced. The term “fiber” as used in the present invention refers to a fiber diameter of 1 μm to 50 μm, a fiber length of 0.1 mm to 30 mm, and a friction material compounding ratio of 40.
A range of less than or equal to wt% is suitable. Above this, there is a trade-off between price and performance, which is not practical.

【0009】従来、ヤシ殻活性炭等の粒状活性炭を摩擦
材に配合した事例はあるが、これらは粒状であるため摩
擦材を製造する際に、内部分布を均一にさせることが難
しく、摩擦クラッチとして作動させると、繊維間より脱
離し、常に安定した摩擦特性を維持することが難しい。
また摩擦係数を高めるため配合比を高めても粒状である
ため、摩擦摺動面では点接触となり摩擦係数を上げる効
果はほとんどない。さらに配合比を高めた場合、繊維間
力が弱まり、摩擦材の強度が低下し、クラッチとして使
用に耐えられるものでなくなる。
Conventionally, there are cases in which granular activated carbon such as coconut shell activated carbon is blended with the friction material, but since these are granular, it is difficult to make the internal distribution uniform when manufacturing the friction material, and as a friction clutch. When actuated, it is detached from between the fibers, and it is difficult to maintain stable friction characteristics at all times.
Further, even if the compounding ratio is increased in order to increase the friction coefficient, the particles are granular, so that point contact occurs on the friction sliding surface and there is almost no effect of increasing the friction coefficient. When the compounding ratio is further increased, the interfiber force is weakened, the strength of the friction material is reduced, and the clutch cannot be used as a clutch.

【0010】また樹脂成分を高めてこの配合比を成立さ
せたとしても、摩擦材の表面が発熱により樹脂成分がプ
ラスチック化(鏡面化)し、摩擦係数が低下するという
不具合がある。これらを解決するために、この発明では
活性炭を繊維とすることによって上記問題をすべて解決
しうるものである。上記湿式摩擦材として抄造タイプの
ものが知られており、その摩擦材は、天然パルプ繊維、
有機合成繊維等を繊維基材とし、これに充填材と摩擦調
整材を配合し抄造して生ペーパーを作り、その生ペーパ
ーに熱硬化性合成樹脂を含侵し乾燥した後、その樹脂を
加熱硬化させることにより、摩擦材を製造している。
Even if the resin component is increased to satisfy this blending ratio, the surface of the friction material is heated and the resin component becomes plastic (mirror-like), resulting in a decrease in the friction coefficient. In order to solve these problems, the present invention can solve all the above problems by using activated carbon as fibers. A paper-making type is known as the wet friction material, and the friction material is a natural pulp fiber,
Organic synthetic fibers are used as a fiber base material, and a filler and a friction modifier are mixed into the raw material to make raw paper. The raw paper is impregnated with a thermosetting synthetic resin and dried, and then the resin is heated and cured. By doing so, the friction material is manufactured.

【0011】熱硬化性合成樹脂は複合繊維紙を構成する
前記繊維等のバインダとして機能し、この種の樹脂とし
ては、フェノール樹脂、エポキシ樹脂、尿素樹脂、メラ
ミン樹脂、シリコン樹脂等が該当する。
The thermosetting synthetic resin functions as a binder for the fibers and the like constituting the composite fiber paper, and as this type of resin, phenol resin, epoxy resin, urea resin, melamine resin, silicone resin and the like are applicable.

【0012】[0012]

【実施例】この発明では、前述の活性炭素繊維を使用す
ることにより、摩擦材が摩擦摺動面に剛性でない弾性を
付与し、摺動面平滑性効果と活性炭繊維の特徴である添
加剤の呼吸作用によって、低温および高温域での摩擦係
数の安定と高摩擦係数の成立、そして高耐熱性の得るこ
とを同時に完成させた新しい発見である。
EXAMPLE In the present invention, by using the above-mentioned activated carbon fiber, the friction material imparts elasticity which is not rigid to the friction sliding surface, and the sliding surface smoothing effect and the additive characteristic of activated carbon fiber are used. It is a new discovery that at the same time completed the achievement of stable coefficient of friction at low and high temperatures, establishment of high coefficient of friction, and high heat resistance by respiration.

【0013】この基礎配合技術の好ましい配合量の範囲
はつぎの通りである。 (好ましい配合例) 天然パルプ・有機合成繊維:20〜60重量% フェノール樹脂 :10〜40重量% 活性炭繊維 : 1〜40重量% 摩擦調整剤・充填剤 : 5〜50重量% この発明は、活性炭繊維を含まないタイプの摩擦材とは
効果に格段の差のある摩擦材を提供するものである。 実施例(L1 それに対して従来例を挙げると、 従来例1(L2 従来例2(L3 製造方法は、上記の配合原料を混合機で均一に混合した
後、抄造装置により抄造した後乾燥し、厚さ0.5mm
の複合繊維紙を得た。次いでこの紙に、上記フェノール
樹脂を含浸させた後フェノール樹脂を硬化させて摩擦材
を製造する。
The preferable range of the compounding amount of this basic compounding technique is as follows. (Preferred compounding example) Natural pulp / organic synthetic fiber: 20-60 wt% Phenolic resin: 10-40 wt% Activated carbon fiber: 1-40 wt% Friction modifier / filler: 5-50 wt% This invention is activated carbon. The fiber-free type friction material provides a friction material having a markedly different effect. Example (L 1 ) On the other hand, the conventional example is the conventional example 1 (L 2 ). Conventional example 2 (L 3 ) The manufacturing method is as follows: After uniformly mixing the above-mentioned blended raw materials with a mixer, paper is made with a paper making device and then dried to have a thickness of 0.5 mm.
The following composite fiber paper was obtained. Then, this paper is impregnated with the above-mentioned phenol resin and then the phenol resin is cured to produce a friction material.

【0014】[0014]

【効果】この発明の摩擦材の効果を調べるために前記の
摩擦材を環状に打ち抜き、鋼板に接着し、テストピース
を作成する。この発明の摩擦材L1 と従来の摩擦材
2 、L3 をそれぞれ図6に示す駆動板2の両面に接合
し、慣性吸収試験機に設けて、間欠的に摩擦係合させた
上で性能比較試験を行った。この試験において、摩擦係
合する時間および休止時間等のモード値は実車テスト同
様の装着されたときと類似した条件を採用した。
[Effect] In order to investigate the effect of the friction material of the present invention, the friction material is punched out in an annular shape and adhered to a steel plate to prepare a test piece. The friction material L 1 of the present invention and the conventional friction materials L 2 and L 3 are joined to both sides of the drive plate 2 shown in FIG. 6, respectively, provided on the inertia absorption tester, and intermittently frictionally engaged. A performance comparison test was conducted. In this test, the mode values such as the friction engagement time and the rest time were similar to those in the actual vehicle test when they were mounted.

【0015】図1は高エネルギー評価による各摩擦材の
耐久寿命を示す。この発明の材質L1 は、比較例で示す
従来材質L2 、L3 と比べて高摩擦係数を維持しながら
安定している。横軸のPV値というのは、スリップトル
クをT、スリップ回転数をNで表したとき、 PV=T・N/1000で示される。
FIG. 1 shows the durable life of each friction material by high energy evaluation. The material L 1 of the present invention is more stable than the conventional materials L 2 and L 3 shown in the comparative example while maintaining a high friction coefficient. When the slip torque is represented by T and the slip rotation number is represented by N, the PV value on the horizontal axis is represented by PV = T · N / 1000.

【0016】図2は、摩擦係合時のショックの指標とな
る回転変化に伴う摩擦係数の変化を示す。この発明の材
質のL1 のみ右上りの勾配を示し、ショックに対し、よ
り有利であることを示している。図3は図1、図2の条
件下における温度変化に伴う摩擦係数の変化を示す。こ
の発明の材質L1 は温度変化に対して大きな反応を示さ
ず、温度環境の変化による摩擦係合装置の容量変化を抑
制することができ、設定容量の安全率を小さくすること
ができ、かつ設定容量と実容量の差である変速ショック
を低減することができる。
FIG. 2 shows a change in friction coefficient with a change in rotation, which is an index of a shock during frictional engagement. Only L 1 of the material of the present invention shows a slope to the upper right, indicating that it is more advantageous against shock. FIG. 3 shows the change of the friction coefficient with the temperature change under the conditions of FIGS. The material L 1 of the present invention does not show a large reaction to the temperature change, can suppress the capacity change of the friction engagement device due to the change of the temperature environment, and can reduce the safety factor of the set capacity, and It is possible to reduce the shift shock, which is the difference between the set capacity and the actual capacity.

【0017】図4はスリップトルク及びスリップ回転数
を種々変化させた場合の摩擦係数の変化を示すもので、
横軸には前述のPV値をとっている。この時の潤滑油温
度は120〜140℃である。図5はこの発明の活性炭
繊維の配合重量%と摩擦係数の関係を示す。大体20〜
30%で一定値となるため、ばらつきを考慮しても、4
0重量%配合すれば最高の摩擦係数を得る目的は達せら
れる。
FIG. 4 shows changes in the friction coefficient when the slip torque and the slip rotation speed are variously changed.
The above-mentioned PV value is taken on the horizontal axis. At this time, the lubricating oil temperature is 120 to 140 ° C. FIG. 5 shows the relationship between the blending weight% of the activated carbon fiber of the present invention and the friction coefficient. 20 ~
Since it is a constant value at 30%, 4
If 0% by weight is blended, the purpose of obtaining the highest friction coefficient can be achieved.

【0018】以上述べたように、この発明によれば、前
記の割合の活性炭繊維を構成材料とすることで、高摩擦
係数、摩擦係数の安定性、及び優秀な耐熱性を備えた湿
式摩擦材を得ることができた。
As described above, according to the present invention, by using the activated carbon fiber in the above proportion as a constituent material, a wet friction material having a high coefficient of friction, stability of the coefficient of friction, and excellent heat resistance is obtained. I was able to get

【図面の簡単な説明】[Brief description of drawings]

【図1】各摩擦材の耐久寿命を示す図である。FIG. 1 is a diagram showing a durable life of each friction material.

【図2】回転変化に伴う摩擦係数の変化を示す図であ
る。
FIG. 2 is a diagram showing a change in a friction coefficient due to a change in rotation.

【図3】温度変化に伴う摩擦係数の変化を示す図であ
る。
FIG. 3 is a diagram showing a change in friction coefficient with a change in temperature.

【図4】PV値を変化させた場合の摩擦係数の変化を示
す図である。
FIG. 4 is a diagram showing changes in the friction coefficient when the PV value is changed.

【図5】活性炭繊維の配合重量%と摩擦係数の関係を示
す図である。
FIG. 5 is a diagram showing a relationship between a blending weight% of activated carbon fibers and a friction coefficient.

【図6】湿式摩擦係合装置の一例の側断面図である。FIG. 6 is a side sectional view of an example of a wet friction engagement device.

【符号の説明】[Explanation of symbols]

1 受動板 2 駆動板 3 プレッシャープレート 4 リテーナ 5 ハブ 6 インプットシャフト 7 押圧ピストン 1 Passive plate 2 Drive plate 3 Pressure plate 4 Retainer 5 Hub 6 Input shaft 7 Pressing piston

─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成5年6月1日[Submission date] June 1, 1993

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0015[Name of item to be corrected] 0015

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0015】図1は高エネルギー評価による各摩擦材の
耐久寿命を示す。この発明の材質L1 は、比較例で示す
従来材質L2 、L3 と比べて高摩擦係数を維持しながら
安定している
FIG. 1 shows the durable life of each friction material by high energy evaluation. The material L 1 of the present invention is more stable than the conventional materials L 2 and L 3 shown in the comparative example while maintaining a high friction coefficient .

【手続補正2】[Procedure Amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0017[Correction target item name] 0017

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0017】図4はスリップトルク及びスリップ回転数
を種々変化させた場合の摩擦係数の変化を示すもので、
横軸にはPV値をとっている。横軸のPV値というの
は、スリップトルクをT、スリップ回転数をNで表した
とき、PV=T・N/1000で示される。この時の潤
滑油温度は120〜140℃である。図5はこの発明の
活性炭繊維の配合重量%と摩擦係数の関係を示す。大体
20〜30%で一定値となるため、ばらつきを考慮して
も、40重量%配合すれば最高の摩擦係数を得る目的は
達せられる。
FIG. 4 shows changes in the friction coefficient when the slip torque and the slip rotation speed are variously changed.
The horizontal axis represents the PV value. The PV value on the horizontal axis
Represents the slip torque by T and the slip rotation speed by N.
At this time, PV = T · N / 1000. At this time, the lubricating oil temperature is 120 to 140 ° C. FIG. 5 shows the relationship between the blending weight% of the activated carbon fiber of the present invention and the friction coefficient. Since it becomes a constant value at about 20 to 30%, the object of obtaining the highest friction coefficient can be achieved by adding 40% by weight even in consideration of variations.

【手続補正3】[Procedure 3]

【補正対象書類名】図面[Document name to be corrected] Drawing

【補正対象項目名】図2[Name of item to be corrected] Figure 2

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【図2】 [Fig. 2]

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 天然パルプ繊維、有機合成繊維等の繊維
基材と、けいそう土、カシュー樹脂等の充填剤や摩擦調
整剤及び熱硬化性合成樹脂を含む摩擦材において、活性
炭繊維を含有することを特徴とする湿式摩擦材。
1. A friction material containing a fibrous base material such as natural pulp fiber or organic synthetic fiber, a filler such as diatomaceous earth or cashew resin, a friction modifier and a thermosetting synthetic resin, and containing activated carbon fiber. A wet friction material characterized by the above.
JP18568592A 1992-06-22 1992-06-22 Wet friction material Expired - Lifetime JP3188311B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP18568592A JP3188311B2 (en) 1992-06-22 1992-06-22 Wet friction material
US08/079,997 US5395864A (en) 1992-06-22 1993-06-18 Wet frictional material containing activated carbon fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18568592A JP3188311B2 (en) 1992-06-22 1992-06-22 Wet friction material

Publications (2)

Publication Number Publication Date
JPH061965A true JPH061965A (en) 1994-01-11
JP3188311B2 JP3188311B2 (en) 2001-07-16

Family

ID=16175078

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Application Number Title Priority Date Filing Date
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Country Status (2)

Country Link
US (1) US5395864A (en)
JP (1) JP3188311B2 (en)

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JPH09194822A (en) * 1996-01-22 1997-07-29 Nissan Motor Co Ltd Wet friction material
KR100327562B1 (en) * 1999-12-29 2002-03-15 양재신 Low noise wet brake disk pad
JP2011516653A (en) * 2008-04-01 2011-05-26 ヴァレオ マトゥリオー ドゥ フリクション Friction material for friction in liquid media, and associated apparatus and method

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FR2717820B1 (en) * 1994-03-25 1996-05-15 Valeo Friction material intended to equip a device implementing friction in a liquid medium, as well as the process for producing such a friction material and the device which is equipped with it.
US6060536A (en) * 1995-01-05 2000-05-09 Nsk-Warner Kabushiki Kaisha Method of producing wet friction material and wet frictional material
US5895716A (en) * 1995-07-18 1999-04-20 The B.F. Goodrich Company Wet friction materials, methods of making them, and apparatus containing the same
US5696198A (en) * 1996-01-22 1997-12-09 Electrosorbent, Inc. Porous electroconductive composite material, and method of manufacturing the same
US6013696A (en) * 1998-01-22 2000-01-11 The Mead Corporation Friction member and method for manufacture thereof
US20050064778A1 (en) * 2003-09-19 2005-03-24 Lam Robert C. High coefficient friction material with symmetrical friction modifying particles
US20050075021A1 (en) * 2003-10-03 2005-04-07 Lam Robert C. High performance, durable, deposit friction material
US7696261B2 (en) * 2003-10-03 2010-04-13 Borgwarner Inc. Mixed deposit friction material
US20050074595A1 (en) * 2003-10-03 2005-04-07 Lam Robert C. Friction material containing partially carbonized carbon fibers
US20050075022A1 (en) * 2003-10-03 2005-04-07 Lam Robert C. Elastic and porous friction material with high amount of fibers
US20050075414A1 (en) * 2003-10-03 2005-04-07 Lam Robert C. High performance, durable, deposit friction material
KR100588342B1 (en) * 2003-11-26 2006-06-12 주식회사 데크 Power transmission clutch
US8021744B2 (en) * 2004-06-18 2011-09-20 Borgwarner Inc. Fully fibrous structure friction material
US7429418B2 (en) 2004-07-26 2008-09-30 Borgwarner, Inc. Porous friction material comprising nanoparticles of friction modifying material
US8603614B2 (en) 2004-07-26 2013-12-10 Borgwarner Inc. Porous friction material with nanoparticles of friction modifying material
US7438839B2 (en) * 2004-10-01 2008-10-21 Honeywell International Inc. Formulation for the manufacture of carbon-carbon composite materials
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JPH09194822A (en) * 1996-01-22 1997-07-29 Nissan Motor Co Ltd Wet friction material
KR100327562B1 (en) * 1999-12-29 2002-03-15 양재신 Low noise wet brake disk pad
JP2011516653A (en) * 2008-04-01 2011-05-26 ヴァレオ マトゥリオー ドゥ フリクション Friction material for friction in liquid media, and associated apparatus and method

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